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Clinical Trials/TCTR20190522001
TCTR20190522001
Completed
Phase 4

A Comparison of Efficacy between Low-Dose Dexmedetomidine and Propofol for Prophylaxis of Postoperative Delirium in Elderly Patients Undergoing Hip Fracture Surgery: A Randomized Controlled Trial

Ratchadapiseksompod fund0 sites108 target enrollmentMay 22, 2019
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ConditionsPostoperative deliriumPostoperative delirium,Dexmedetomidine, Propofol,Hip surgery

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Postoperative delirium
Sponsor
Ratchadapiseksompod fund
Enrollment
108
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 22, 2019
End Date
April 30, 2021
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Ratchadapiseksompod fund

Eligibility Criteria

Inclusion Criteria

  • •Age 60 years old or older
  • •\- Admit post\-operative in ICU
  • •\- Closed fracture intertrochanteric or neck of femur
  • •\- ASA (American Society of Anesthesiologists) class 2\-3
  • •\- BMI 18 \- 40 kg/m2

Exclusion Criteria

  • •\- Patient refusal
  • •\- Allergy to drugs used in this research
  • •\- Richmond Agitation Sedation Scale (RASS) less than \- 2 before sedation
  • •\- Prior delirium or dementia
  • •\- Prior or acute cerebrovascular disease
  • •\- Bradycardia eg. Second or Third\-degree atrioventricular block
  • •\- Prior temporary or permanent pacemaker
  • •\- Bradycardia (HR less than 50 bpm) of different origin
  • •\- Severe congestive heart failure
  • •\- Obstructive sleep apnea

Outcomes

Primary Outcomes

Not specified

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